SI3154950T1 - Hidrokloridne soli N-(cianometil)-4-(2-(4-morfolinofenilamino)pirimidin-4-il)benzamida - Google Patents

Hidrokloridne soli N-(cianometil)-4-(2-(4-morfolinofenilamino)pirimidin-4-il)benzamida

Info

Publication number
SI3154950T1
SI3154950T1 SI201531370T SI201531370T SI3154950T1 SI 3154950 T1 SI3154950 T1 SI 3154950T1 SI 201531370 T SI201531370 T SI 201531370T SI 201531370 T SI201531370 T SI 201531370T SI 3154950 T1 SI3154950 T1 SI 3154950T1
Authority
SI
Slovenia
Prior art keywords
morpholinophenylamino
cyanomethyl
pyrimidin
benzamide hydrochloride
hydrochloride salts
Prior art date
Application number
SI201531370T
Other languages
English (en)
Slovenian (sl)
Inventor
Brandon H. Brown
Ernest A. Carra
Jeffrey N. Hemenway
Henry Morrison
Troy Reynolds
Bing Shi
Dimitrios Stefanidis
Fang Wang
Matthew Robert Warr
James Andrew Whitney
Yan Xin
Original Assignee
Sierra Oncology, Inc.,
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=53674249&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SI3154950(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sierra Oncology, Inc., filed Critical Sierra Oncology, Inc.,
Publication of SI3154950T1 publication Critical patent/SI3154950T1/sl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/281,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/301,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
SI201531370T 2014-06-12 2015-06-11 Hidrokloridne soli N-(cianometil)-4-(2-(4-morfolinofenilamino)pirimidin-4-il)benzamida SI3154950T1 (sl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462011315P 2014-06-12 2014-06-12
EP15739042.8A EP3154950B1 (en) 2014-06-12 2015-06-11 N-(cyanomethyl)-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide hydrochloride salts
PCT/US2015/035316 WO2015191846A1 (en) 2014-06-12 2015-06-11 N-(cyanomethyl)-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide hydrochloride salts

Publications (1)

Publication Number Publication Date
SI3154950T1 true SI3154950T1 (sl) 2021-01-29

Family

ID=53674249

Family Applications (1)

Application Number Title Priority Date Filing Date
SI201531370T SI3154950T1 (sl) 2014-06-12 2015-06-11 Hidrokloridne soli N-(cianometil)-4-(2-(4-morfolinofenilamino)pirimidin-4-il)benzamida

Country Status (33)

Country Link
US (4) US9469613B2 (el)
EP (3) EP3719005A1 (el)
JP (5) JP6600649B2 (el)
KR (1) KR101928225B1 (el)
CN (2) CN106458929A (el)
AP (1) AP2016009551A0 (el)
AR (1) AR100818A1 (el)
AU (1) AU2015274554B9 (el)
BR (1) BR112016028749A2 (el)
CA (1) CA2951883C (el)
CR (1) CR20160575A (el)
CU (1) CU20160183A7 (el)
CY (1) CY1123604T1 (el)
DK (1) DK3154950T3 (el)
EA (1) EA032639B1 (el)
EC (1) ECSP16093323A (el)
ES (1) ES2822773T3 (el)
HR (1) HRP20201492T1 (el)
HU (1) HUE051360T2 (el)
IL (3) IL249038B (el)
LT (1) LT3154950T (el)
MA (1) MA40067A (el)
MX (3) MX2016016294A (el)
NZ (1) NZ725966A (el)
PH (1) PH12016502461A1 (el)
PL (1) PL3154950T3 (el)
PT (1) PT3154950T (el)
RS (1) RS61065B1 (el)
SG (2) SG10201911925TA (el)
SI (1) SI3154950T1 (el)
TW (3) TW202134236A (el)
UY (1) UY36166A (el)
WO (1) WO2015191846A1 (el)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW202134236A (zh) 2014-06-12 2021-09-16 美商西爾拉癌症醫學公司 N-(氰基甲基)-4-(2-(4-𠰌啉基苯基胺基)嘧啶-4-基)苯甲醯胺
CN106316964B (zh) * 2015-06-26 2019-06-25 苏州泽璟生物制药股份有限公司 苯基氨基嘧啶化合物或其盐的多晶型物
CN106316963B (zh) * 2015-06-26 2021-06-08 苏州泽璟生物制药股份有限公司 吗啡啉苯基氨基嘧啶化合物或其盐的多晶型物
TWI808055B (zh) 2016-05-11 2023-07-11 美商滬亞生物國際有限公司 Hdac 抑制劑與 pd-1 抑制劑之組合治療
TWI794171B (zh) 2016-05-11 2023-03-01 美商滬亞生物國際有限公司 Hdac抑制劑與pd-l1抑制劑之組合治療
US10245268B2 (en) 2016-08-10 2019-04-02 Sierra Oncology, Inc. Treatment of ACVR1-mediated diseases
JP2021523882A (ja) * 2018-05-15 2021-09-09 ジエンス ハンセン ファーマセウティカル グループ カンパニー リミテッド 低分子egfr阻害剤を含む医薬組成物及びその製造方法
US11963962B2 (en) 2018-08-21 2024-04-23 Glaxosmithkline Llc Platelet count-agnostic methods of treating myelofibrosis
EP3923948A4 (en) * 2019-02-12 2022-11-16 Impact Biomedicines, Inc. CRYSTALLINE SHAPES OF A JAK2 INHIBITOR
WO2023010111A1 (en) 2021-07-30 2023-02-02 Sierra Oncology, Inc. Biomarker and patient selection in treatment for myelofibrosis
CN117794546A (zh) 2021-08-10 2024-03-29 葛兰素史密斯克莱有限责任公司 莫洛替尼组合疗法
WO2023023473A1 (en) 2021-08-16 2023-02-23 Sierra Oncology, Inc. Methods of using momelotinib to treat chronic kidney disease
WO2023152773A1 (en) * 2022-02-14 2023-08-17 Dr. Reddy's Institute Of Life Sciences Solid forms of momelotinib salts and improved processes for the preparation of momelotinib

Family Cites Families (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3481932A (en) 1967-09-01 1969-12-02 Searle & Co 2-anilino-5-methyl-6-phenylpyrimidines and congeners
US5021456A (en) 1988-02-25 1991-06-04 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US4965288A (en) 1988-02-25 1990-10-23 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US5252608A (en) 1988-02-25 1993-10-12 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US5059714A (en) 1988-02-25 1991-10-22 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US5182297A (en) 1988-02-25 1993-01-26 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US4943593A (en) 1988-02-25 1990-07-24 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US5120764A (en) 1988-11-01 1992-06-09 Merrell Dow Pharmaceuticals Inc. Inhibitors of lysyl oxidase
US4997854A (en) 1989-08-25 1991-03-05 Trustees Of Boston University Anti-fibrotic agents and methods for inhibiting the activity of lysyl oxidase in-situ using adjacently positioned diamine analogue substrates
US5559714A (en) 1990-10-22 1996-09-24 Hallmark Cards, Incorporated Method and apparatus for display sequencing personalized social occasion products
GB9523675D0 (en) 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
GB9914258D0 (en) 1999-06-18 1999-08-18 Celltech Therapeutics Ltd Chemical compounds
GB9924862D0 (en) 1999-10-20 1999-12-22 Celltech Therapeutics Ltd Chemical compounds
US7122544B2 (en) 2000-12-06 2006-10-17 Signal Pharmaceuticals, Llc Anilinopyrimidine derivatives as IKK inhibitors and compositions and methods related thereto
CA2436487A1 (en) 2001-01-30 2002-08-08 Cytopia Pty Ltd. Methods of inhibiting kinases
MXPA03008888A (es) 2001-03-29 2005-03-07 Vertex Pharma Inhibidores de n-terminal c-jun cinasas (jnk) y otras proteinas cinasas.
FR2828206B1 (fr) 2001-08-03 2004-09-24 Centre Nat Rech Scient Utilisation d'inhibiteurs des lysyl oxydases pour la culture cellulaire et le genie tissulaire
US6433018B1 (en) 2001-08-31 2002-08-13 The Research Foundation Of State University Of New York Method for reducing hypertrophy and ischemia
DE60227538D1 (de) 2001-09-12 2008-08-21 Virexx Medical Corp Festphasenmittel zur vaskulären okklusion mit immo
DE60317198T2 (de) 2002-05-23 2008-12-04 Cytopia Research Pty. Ltd., Richmond Proteinkinaseinhibitoren
WO2004016597A2 (en) 2002-08-14 2004-02-26 Vertex Pharmaceuticals Incorporated Protein kinase inhibitors and uses thereof
JP2006512314A (ja) 2002-11-01 2006-04-13 バーテックス ファーマシューティカルズ インコーポレイテッド Jakインヒビターおよび他のプロテインキナーゼインヒビターとしての組成物の使用
AU2003295396B2 (en) 2002-11-04 2009-02-26 Vertex Pharmaceuticals Incorporated Heteroaryl-pyramidine derivatives as JAK inhibitors
CA2507406A1 (en) 2002-11-05 2004-05-21 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of jak and other protein kinases
GB0317841D0 (en) 2003-07-30 2003-09-03 Cyclacel Ltd Compound
AU2004261484A1 (en) 2003-07-30 2005-02-10 Cyclacel Limited 2-aminophenyl-4-phenylpyrimidines as kinase inhibitors
CA2566609C (en) 2004-05-13 2012-06-26 Icos Corporation Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta
AR051387A1 (es) 2004-10-13 2007-01-10 Wyeth Corp Analogos de anilino-pirimidina
US7593820B2 (en) 2005-05-12 2009-09-22 Cytopia Research Pty Ltd Crystal structure of human Janus Kinase 2 (JAK2) and uses thereof
JP2009525337A (ja) 2006-01-30 2009-07-09 エクセリクシス, インク. Jak−2調節因子としての4−アリール−2−アミノ−ピリミジン類又は4−アリール−2−アミノアルキル−ピリミジン類と使用方法
WO2007101232A2 (en) 2006-02-28 2007-09-07 Cytopia Research Pty, Ltd. Inhibition of jak2 as a treatment of pulmonary arterial hypertension
FR2911139A1 (fr) 2007-01-05 2008-07-11 Sanofi Aventis Sa Nouveaux derives de phenyl-(4-phenyl-pyrimidin-2-yl)amines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
AU2013201306B2 (en) 2007-03-12 2015-11-12 Glaxosmithkline Llc Phenyl Amino Pyrimidine Compounds and Uses Thereof
DK2152701T3 (en) 2007-03-12 2016-02-15 Ym Biosciences Australia Pty Phenylaminopyrimidinforbindelser and uses thereof
AU2016200866B2 (en) 2007-03-12 2017-06-22 Glaxosmithkline Llc Phenyl amino pyrimidine compounds and uses thereof
PT2200436E (pt) 2007-09-04 2015-04-29 Scripps Research Inst Pirimidinilaminas substituídas como inibidoras da proteína quinase
WO2009029998A1 (en) 2007-09-06 2009-03-12 Cytopia Research Pty Ltd Retrometabolic compounds
US20100310563A1 (en) 2007-11-30 2010-12-09 Bumm Thomas G P Methods for treating induced cellular proliferative disorders
BRPI0917575A2 (pt) 2008-08-05 2019-09-24 Targegen Inc métodos de tratamento de talassemia
UA102128C2 (en) 2008-12-05 2013-06-10 Х. Луннбек А/С Nalmefene hydrochloride dihydrate
US8450321B2 (en) 2008-12-08 2013-05-28 Gilead Connecticut, Inc. 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
WO2010141946A1 (en) 2009-06-05 2010-12-09 Cell Targeting, Inc. Peptide-coated cell localization to diseased or damaged tissues and methods related thereto
JP5086385B2 (ja) * 2010-03-08 2012-11-28 日立オートモティブシステムズ株式会社 電動パワーステアリング制御装置
MX2012013622A (es) 2010-05-31 2013-02-01 Ono Pharmaceutical Co Derivado de purinona.
NZ611654A (en) * 2010-12-03 2015-08-28 Ym Biosciences Australia Pty Treatment of jak2-mediated conditions
BR112013028420A2 (pt) 2011-05-02 2017-01-24 Ym Biosciences Australia Pty tratamento de mieloma múltiplo
US8809359B2 (en) 2012-06-29 2014-08-19 Ym Biosciences Australia Pty Ltd Phenyl amino pyrimidine bicyclic compounds and uses thereof
JPWO2014051056A1 (ja) * 2012-09-28 2016-08-22 東レ株式会社 グリシン誘導体の結晶及びその医薬用途
EP2943489B1 (en) 2013-01-09 2018-04-11 Concert Pharmaceuticals Inc. Deuterated momelotinib
CN103965114B (zh) 2013-01-28 2016-01-06 苏州泽璟生物制药有限公司 氘代的苯基氨基嘧啶化合物以及包含该化合物的药物组合物
TW202134236A (zh) 2014-06-12 2021-09-16 美商西爾拉癌症醫學公司 N-(氰基甲基)-4-(2-(4-𠰌啉基苯基胺基)嘧啶-4-基)苯甲醯胺

Also Published As

Publication number Publication date
MX2019009564A (es) 2019-10-02
JP2021107465A (ja) 2021-07-29
MX2022015558A (es) 2023-01-30
USRE49445E1 (en) 2023-03-07
CA2951883C (en) 2020-05-05
JP7198867B2 (ja) 2023-01-04
PL3154950T3 (pl) 2021-01-25
MA40067A (fr) 2015-12-17
JP6840909B2 (ja) 2021-03-10
ES2822773T3 (es) 2021-05-04
TWI681954B (zh) 2020-01-11
IL276948A (en) 2020-10-29
TW202134236A (zh) 2021-09-16
EP3907219A1 (en) 2021-11-10
WO2015191846A1 (en) 2015-12-17
LT3154950T (lt) 2020-11-25
CA2951883A1 (en) 2015-12-17
TW202012378A (zh) 2020-04-01
KR20170015496A (ko) 2017-02-08
NZ725966A (en) 2018-04-27
EP3154950B1 (en) 2020-08-05
EA032639B1 (ru) 2019-06-28
AU2015274554A1 (en) 2016-11-24
US9809559B2 (en) 2017-11-07
AR100818A1 (es) 2016-11-02
CN106458929A (zh) 2017-02-22
UY36166A (es) 2016-01-29
SG10201911925TA (en) 2020-01-30
AU2015274554B2 (en) 2018-02-15
JP2020059759A (ja) 2020-04-16
MX2016016294A (es) 2017-09-01
HRP20201492T1 (hr) 2021-01-08
AP2016009551A0 (en) 2016-11-30
ECSP16093323A (es) 2017-01-31
CY1123604T1 (el) 2022-03-24
IL249038A0 (en) 2017-01-31
PT3154950T (pt) 2020-10-09
JP2017517535A (ja) 2017-06-29
CR20160575A (es) 2017-01-20
DK3154950T3 (da) 2020-09-14
JP2018184486A (ja) 2018-11-22
US20160347719A1 (en) 2016-12-01
PH12016502461A1 (en) 2017-03-06
SG11201610079VA (en) 2016-12-29
KR101928225B1 (ko) 2018-12-11
USRE48285E1 (en) 2020-10-27
US20150361050A1 (en) 2015-12-17
IL276948B (en) 2021-09-30
CN110627728A (zh) 2019-12-31
US9469613B2 (en) 2016-10-18
IL286442A (en) 2021-10-31
RS61065B1 (sr) 2020-12-31
JP6883560B2 (ja) 2021-06-09
TW201617323A (zh) 2016-05-16
JP2023021454A (ja) 2023-02-10
JP6600649B2 (ja) 2019-10-30
EA201692356A1 (ru) 2017-07-31
EP3719005A1 (en) 2020-10-07
CU20160183A7 (es) 2017-05-10
BR112016028749A2 (pt) 2017-08-22
AU2015274554B9 (en) 2018-04-19
TWI729644B (zh) 2021-06-01
HUE051360T2 (hu) 2021-03-01
EP3154950A1 (en) 2017-04-19
IL249038B (en) 2020-09-30

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